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Research Progress on Plutonium Adsorption Behavior

Authors :
ZHANG Ye
LI Xiang
WANG Wen-tao
Source :
He huaxue yu fangshe huaxue, Vol 46, Iss 1, Pp 37-45 (2024)
Publication Year :
2024
Publisher :
Editorial Office of Journal of Nuclear and Radiochemistry, 2024.

Abstract

Plutonium(Pu) is a very critical radioactive element, and its separation and purification are the core technology in the reprocessing of spent fuel. At the same time, research on the separation of Pu is also of great significance to environmental protection and radioactive pollution remediation. Currently, precipitation, extraction, and adsorption are the primary techniques for separating and purifying plutonium. Of these, adsorption is a crucial method for the process. The technique offers benefits such as simplicity of operation and high-speed adsorption. Additionally, adsorbents have advantages in the form of low cost and high adsorption capacity. In the review, according to the properties of adsorption materials, we introduced the research progress on the adsorption and separation of Pu from five aspects: natural mineral, polymer resins, inorganic oxides, carbon materials and nanomaterials. Furthermore, the adsorption ability and mechanisms of these different adsorption materials as well as the influencing factors during the adsorption process were also summarized and discussed. Based on these discussions, the advantages and disadvantages of these different materials were also evaluated. Finally, the problems and future development trend of the plutonium adsorption and separation were analyzed and prospected, which should be provided guidance for the research and application in the adsorption and separation of Pu and other radionuclides.

Details

Language :
Chinese
ISSN :
02539950
Volume :
46
Issue :
1
Database :
Directory of Open Access Journals
Journal :
He huaxue yu fangshe huaxue
Publication Type :
Academic Journal
Accession number :
edsdoj.0f4dbf1b7504443ca291c287f83f5a0c
Document Type :
article
Full Text :
https://doi.org/10.7538/hhx.2024.46.01.0037